Author

Noah Copperman

Albert Einstein College of MedicineORCID 0009-0005-1450-3412Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cancer & tumor microenvironment· 2 Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

David Mark LoebiD· 2 shared Alexander Forrest· 1 shared Antonio Di CristofanoiD· 1 shared Avital Adah RodaliD· 1 shared Bing XuiD· 1 shared Chaoshuang XiaiD· 1 shared Cheng Lin· 1 shared Daniela M. DinulescuiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersBiochemistry

David Mark LoebORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

BiochemistryNature CommunicationsPeer-reviewedJan 28, 2026

Cycling Molecular Assemblies for Selective Cancer Cell Golgi Disruption

Weiyi Tan, Qiuxin Zhang, Zhiyu Liu…·Bing Xu

This paper develops CyMA, small peptides that disrupt cancer cell Golgi function by exploiting enzymatic cycles, showing selectivity over hepatocytes and immune cells.

6 citations

humanexperimental assay

𝕏 PostBluesky

Cancer BiologybioRxivPreprintApr 13, 2025

Inhibition Of One-Carbon Metabolism In Ewing Sarcoma Results In Profound And Prolonged Growth Suppression Associated With Purine Depletion

Sara Zirpoli, Noah Copperman, Shrey D. Patel…·Antonio Di Cristofano

This study shows that inhibiting one-carbon metabolism in Ewing sarcoma cells leads to growth suppression through purine depletion, identifying a potential therapeutic target.

DOI 10.1101/2025.04.13.647987

humanbulk RNA-seq

𝕏 PostBluesky